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Download Hi-Res ImageDownload to MS-PowerPointCite This:J. Org. Chem. 2011, 76, 3, 990-992
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    Axially Chiral Bichromophoric Fluorescent Dyes
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    † Department of Chemistry, LMU University of Munich, Butenandtstrasse 13, D-81377 Munich, Germany
    ‡ Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States
    § Institute of Organic Chemistry, University of Zuerich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland
    [email protected]
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    The Journal of Organic Chemistry

    Cite this: J. Org. Chem. 2011, 76, 3, 990–992
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    https://doi.org/10.1021/jo102254a
    Published January 13, 2011
    Copyright © 2011 American Chemical Society
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    Abstract

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    A new life for Kurt Mislow’s authentic amines: Diaminobiphenyls were applied as the framework materials for the synthesis of axially chiral bichromophoric systems with strong CD and CPL effects.

    Copyright © 2011 American Chemical Society

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    Supporting Information

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    Crystallographic data of (M)-1, 1H NMR and 13C NMR of compounds (M)-1, (P)-4, and (M)-4, the measurement of the fluorescence lifetime of (M)-4, stability of the configuration of (P)-4, and the thermal stability of (P)-4 by DTA (differential thermoanalysis) and TGA (thermogravimetry). This material is available free of charge via the Internet at http://pubs.acs.org.

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    The Journal of Organic Chemistry

    Cite this: J. Org. Chem. 2011, 76, 3, 990–992
    Click to copy citationCitation copied!
    https://doi.org/10.1021/jo102254a
    Published January 13, 2011
    Copyright © 2011 American Chemical Society
    Request reuse permissions

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